Cas 145371-52-4,5-<p-(phenylthio)phenyl>-1-ethyl-5-methyldihydro-<1H,7H>-5H-pyrano<3,2-d>oxazole-2,6-dione

145371-52-4

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Basic information

Product Name: 5--1-ethyl-5-methyldihydro-<1H,7H>-5H-pyrano<3,2-d>oxazole-2,6-dione
Synonyms: 5--1-ethyl-5-methyldihydro-<1H,7H>-5H-pyrano<3,2-d>oxazole-2,6-dione
CAS NO:145371-52-4
Molecular Formula:
Molecular Weight: 383.468
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5--1-ethyl-5-methyldihydro-<1H,7H>-5H-pyrano<3,2-d>oxazole-2,6-dione(CAS DataBase Reference)
NIST Chemistry Reference: 5--1-ethyl-5-methyldihydro-<1H,7H>-5H-pyrano<3,2-d>oxazole-2,6-dione(145371-52-4)
EPA Substance Registry System: 5--1-ethyl-5-methyldihydro-<1H,7H>-5H-pyrano<3,2-d>oxazole-2,6-dione(145371-52-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 145371-52-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 145371-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,3,7 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 145371-52:
(8*1)+(7*4)+(6*5)+(5*3)+(4*7)+(3*1)+(2*5)+(1*2)=124
124 % 10 = 4
So 145371-52-4 is a valid CAS Registry Number.

145371-52-4Upstream product

145371-52-4Downstream Products

145371-64-8 1-ethyl-5-methyl-5--6-hydroxyperhydropyrano<3,2-d>oxazole-2-one

145371-52-4Relevant academic research and scientific papers

Synthesis and antimicrobial properties of 2H-pyran-3(6H)-one derivatives and related compounds

Georgiadis,Couladouros,Delitheos

, p. 1126 - 1131 (2007/10/02)

The synthesis of several derivatives of 2H-pyran-3(6H)-ones and their Michael adducts is described. Phenylthio, benzenesulfonyl, p- acetylaminobenzenesulfonyl, and p-bromophenyl substituents are beneficial for activity against gram-positive bacteria. 2-[4

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